(Q34663411)

3 August 2017

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title

Brain malformations, epilepsy, and infantile spasms (English)

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3 August 2017

M Elizabeth Ross

1

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3 August 2017

publication date

1 January 2002

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International Review of Neurobiology

3 August 2017

published in

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3 August 2017

volume

49

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3 August 2017

page(s)

333-352

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Non-progressive familial congenital cerebellar hypoplasia

3 August 2017

cites work

1 reference

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7 January 2021

Electrophysiology of CA1 pyramidal neurons in an animal model of neuronal migration disorders: prenatal methylazoxymethanol treatment

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7 January 2021

Characterization of heterotopic cell clusters in the hippocampus of rats exposed to methylazoxymethanol in utero.

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7 January 2021

Platelet-activating factor receptor stimulation disrupts neuronal migration In vitro.

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7 January 2021

Bilateral perisylvian polymicrogyria in three generations.

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7 January 2021

Spatial and temporal development of the gliovascular tissue in type II lissencephaly

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7 January 2021

Reelin regulates the development and synaptogenesis of the layer-specific entorhino-hippocampal connections.

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7 January 2021

Development of commissural connections in the hippocampus of reeler mice: evidence of an inhibitory influence of Cajal-Retzius cells.

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7 January 2021

Petit mal epilepsy and parkinsonian tremor: hypothesis of a common pacemaker

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7 January 2021

Neocortical histogenesis in normal and reeler mice: a developmental study based upon [3H]thymidine autoradiography.

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7 January 2021

Mechanisms of Cortical Development: A View From Mutations in Mice

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7 January 2021

Distribution and initiation of seizure activity in a rat brain with subcortical band heterotopia

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7 January 2021

The right neuron at the wrong place: biology of heterotopic neurons in cortical neuronal migration disorders, with special reference to associated pathologies.

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7 January 2021

Abnormal connections in the malformed cortex of rats with prenatal treatment with methylazoxymethanol may support hyperexcitability

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7 January 2021

Cortical malformations and epilepsy: new insights from animal models

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7 January 2021

Neocortex in the hippocampus: an anatomical and functional study of CA1 heterotopias after prenatal treatment with methylazoxymethanol in rats.

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7 January 2021

Ictal patterns of cerebral glucose utilization in children with epilepsy

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7 January 2021

Thalamocortical rhythm generation in vitro: extra- and intracellular recordings in mouse thalamocortical slices perfused with low Mg2+ medium

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7 January 2021

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7 January 2021

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

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7 January 2021

Increased presynaptic protein kinase C activity and glutamate release in rats with a prenatally induced hippocampal lesion.

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7 January 2021

X-linked malformations of neuronal migration

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7 January 2021

Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13.

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7 January 2021

Lissencephaly and other malformations of cortical development: 1995 update

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7 January 2021

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7 January 2021

LIS1 regulates CNS lamination by interacting with mNudE, a central component of the centrosome

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7 January 2021

Hippocampal abnormalities and enhanced excitability in a murine model of human lissencephaly

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7 January 2021

Folding of proteins with WD-repeats: comparison of six members of the WD-repeat superfamily to the G protein beta subunit

1 reference

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7 January 2021

Developmental aspects of type II lissencephaly. Comparative study of dysplastic lesions in fetal and post-natal brains.

1 reference

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7 January 2021

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Characterization of mutations in the gene doublecortin in patients with double cortex syndrome

1 reference

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7 January 2021

Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Bilateral frontal polymicrogyria: a newly recognized brain malformation syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Immunohistochemical analysis of brainstem lesions in infantile spasms

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Brain acetylhydrolase that inactivates platelet-activating factor is a G-protein-like trimer

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Focal epileptogenesis in a rat model of polymicrogyria

1 reference

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7 January 2021

Histological and neurochemical effects of fetal treatment with methylazoxymethanol on rat neocortex in adulthood

1 reference

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7 January 2021

Diffuse pachygyria with cerebellar hypoplasia: a milder form of microlissencephaly or a new genetic syndrome?

1 reference

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7 January 2021

Direct association of LIS1, the lissencephaly gene product, with a mammalian homologue of a fungal nuclear distribution protein, rNUDE

1 reference

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7 January 2021

Heterotopic neurogenesis in a rat with cortical heterotopia.

1 reference

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7 January 2021

A genetic animal model of human neocortical heterotopia associated with seizures

1 reference

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7 January 2021

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia

1 reference

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7 January 2021

Sleep and arousal: thalamocortical mechanisms

1 reference

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7 January 2021

Interactions between sleep and epilepsy

1 reference

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7 January 2021

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Cell migration from the ganglionic eminences is required for the development of hippocampal GABAergic interneurons

1 reference

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7 January 2021

Differential downregulation of GABAA receptor subunits in widespread brain regions in the freeze-lesion model of focal cortical malformations.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Human brain malformations and their lessons for neuronal migration

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Lissencephaly with cerebellar hypoplasia (LCH): a heterogeneous group of cortical malformations

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

LIS1 is a microtubule-associated phosphoprotein

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Reduction of microtubule catastrophe events by LIS1, platelet-activating factor acetylhydrolase subunit.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Reelin mRNA expression during mouse brain development

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Subcortical connections of normotopic and heterotopic neurons in sensory and motor cortices of the tish mutant rat.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Abnormal reorganization of preplate neurons and their associated extracellular matrix: an early manifestation of altered neocortical development in the reeler mutant mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Regulation of cytoplasmic dynein behaviour and microtubule organization by mammalian Lis1

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Lissencephaly associated mutations suggest a requirement for the PAFAH1B heterotrimeric complex in brain development

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Bilateral frontoparietal polymicrogyria and epilepsy.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Patient mutations in doublecortin define a repeated tubulin-binding domain

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Cortical target depletion and ingrowth of geniculocortical axons: implications for cortical specification.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

NudF, a nuclear migration gene in Aspergillus nidulans, is similar to the human LIS-1 gene required for neuronal migration

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

Anticonvulsant drug effects on spontaneous thalamocortical rhythms in vitro: phenytoin, carbamazepine, and phenobarbital

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2802%2949020-4

7 January 2021

10.1016/S0074-7742(02)49020-4

Identifiers

DOI

1 reference

3 August 2017

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